Top 25 Fda consulting firms based in the Netherlands

“PCS helps pharmaceutical and biotech organisations turn compliance into a performance advantage.”

“Qserve is a trusted global partner for MedTech Regulatory, Clinical, and Quality Compliance, as well as a full-service CRO for medical device clinical trials.”

“Progress – Experts in Life Sciences is a Life Sciences consulting partner for pharma, biotech and healthcare organizations in The Netherlands.”

“Interdos is part of the Basic Pharma Group located at the Brightlands Chemelot Campus in Geleen, the Netherlands.”

“Zwiers Regulatory Consultancy, now part of ProductLife Group, offers end-to-end regulatory support from early development to post-marketing compliance.”

“CR2O is a full-service Contract Research Organization.”

“By sharing expertise, infrastructure and equipment, we improve product quality, increase efficiency and reduce costs.”

“Starodub BV is a team of expert consultants in Regulatory Affairs, Quality, Operations & Improvement.”

“Depending on your needs we can act at different process levels in your organization e.g.”

“Regulatory & Quality Compliance Medical Technologies Services, enabling Global Market Access- MedTech: EU-MDR – US-FDA Compliance – High (Innovative) Risk (Implants), Combination…”

“RegPak BioPharma is an Amsterdam based full service Regulatory Affairs Consultancy with the key objective of providing high quality services within Regulatory Affairs, Licensing…”

“Neunco Pharmaceuticals is an established consultancy firm that represents exceptional clinical trial distribution and pharma companies, our journey began by providing…”

“We’ve moved!”

“Zentis is the Leading Software Partner for MDR/FDA-Compliant Medical Device Manufacturers.”

“To implement and execute the complete process with the big variety of tasks, complexity and the amount of work, it is possible some additional hands are required in your team.”

“R-S-S was launched with the aim of supporting the Biopharma industry by offering unparalleled scientific data solutions and consultancy centred around our regulatory expertise.”

“CREATE is a regulatory consultancy specializing in medical device regulations, including EU MDR, IVDR, FDA, and Health Canada requirements.”

“Geronimo Consultancy provides advise and support on many aspects of clinical and pharmaceutical development.”

“We are a regulatory consulting firm in the Netherlands with expertise in food products (conventional foods, fortified foods, food supplements, foods for specific groups) and…”

“Groots Medical Device Expert is your excellence consultant to ensure market access of safe medical devices, which perform as intended, through compliance with the applicable…”